UQCC2 (GeneID: 84300) | Homo sapiens
Description: ubiquinol-cytochrome c reductase complex assembly factor 2 [Source:HGNC Symbol;Acc:HGNC:21237]
Synonyms: Cbp6, bA6B20.2, NF1, C6orf126, M19, C6orf125
Other ID(s): HGNC:21237, ENSG00000137288
Protein Accession Numbers: ENST00000374214, ENST00000607484.1, ENST00000607484, ENST00000374231, NP_115716
Statistics: gnomAD(82) COSMIC(58)
gnomAD Variants By Annotation
6%2%60%1%2%4%24%10010090908080707060605050404030302020101000
Frameshift Variant
Inframe Deletion
Missense Variant
Splice Region Variant
Start Lost
Stop Gained
Synonymous Variant
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∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000374214 You are here now! ENST00000374231 ENST00000607484 NP_115716


healinggnomAD
6%2%60%1%2%4%24%10010090908080707060605050404030302020101000
Frameshift Variant
Inframe Deletion
Missense Variant
Splice Region Variant
Start Lost
Stop Gained
Synonymous Variant
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blur_onCatalogue of Somatic Mutations in Cancer (COSMIC)
3%12%16%3%66%10010090908080707060605050404030302020101000
Deletion - Frameshift
Substitution - Coding Silent
Substitution - Missense
Substitution - Nonsense
Unknown
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format_align_centerProtein Domains (PFAM)
Pfam Domain filter_list Domain Name filter_list Description filter_list Positions filter_list Clan filter_list Clan Name filter_list Organism filter_list
NO RESULT FOUND
NO DOMAINS EXIST

view_listList of the diseases from DisGeNET
Disease Name filter_list Disease Category filter_list DSI* filter_list DPI** filter_list
Ubiquinone dehydrogenase deficiency N/A 0.743 0.345
Mitochondrial Diseases Nutritional and Metabolic Diseases ; 0.743 0.345
MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder) Nutritional and Metabolic Diseases ; 0.743 0.345
NO RESULT FOUND
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